JP2000504722A5 - - Google Patents

Download PDF

Info

Publication number
JP2000504722A5
JP2000504722A5 JP1997529318A JP52931897A JP2000504722A5 JP 2000504722 A5 JP2000504722 A5 JP 2000504722A5 JP 1997529318 A JP1997529318 A JP 1997529318A JP 52931897 A JP52931897 A JP 52931897A JP 2000504722 A5 JP2000504722 A5 JP 2000504722A5
Authority
JP
Japan
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
JP1997529318A
Other languages
English (en)
Japanese (ja)
Other versions
JP2000504722A (ja
Filing date
Publication date
Priority claimed from PCT/US1996/002260 external-priority patent/WO1996025157A1/fr
Application filed filed Critical
Publication of JP2000504722A publication Critical patent/JP2000504722A/ja
Publication of JP2000504722A5 publication Critical patent/JP2000504722A5/ja
Withdrawn legal-status Critical Current

Links

JP9529318A 1995-02-17 1996-08-21 Il―8レセプターアンタゴニスト Withdrawn JP2000504722A (ja)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US39026095A 1995-02-17 1995-02-17
WO96/02260 1996-02-16
PCT/US1996/002260 WO1996025157A1 (fr) 1995-02-17 1996-02-16 Antagonistes des recepteurs d'il-8
PCT/US1996/013632 WO1997029743A1 (fr) 1995-02-17 1996-08-21 Antagonistes de recepteurs de l'interleukine-8

Publications (2)

Publication Number Publication Date
JP2000504722A JP2000504722A (ja) 2000-04-18
JP2000504722A5 true JP2000504722A5 (fr) 2004-09-16

Family

ID=23541762

Family Applications (2)

Application Number Title Priority Date Filing Date
JP8525199A Withdrawn JPH11503110A (ja) 1995-02-17 1996-02-16 Il−8受容体拮抗剤
JP9529318A Withdrawn JP2000504722A (ja) 1995-02-17 1996-08-21 Il―8レセプターアンタゴニスト

Family Applications Before (1)

Application Number Title Priority Date Filing Date
JP8525199A Withdrawn JPH11503110A (ja) 1995-02-17 1996-02-16 Il−8受容体拮抗剤

Country Status (19)

Country Link
US (2) US5886044A (fr)
EP (2) EP0809492A4 (fr)
JP (2) JPH11503110A (fr)
KR (1) KR19990082622A (fr)
CN (2) CN1539816A (fr)
AU (1) AU725456B2 (fr)
BG (1) BG102690A (fr)
BR (1) BR9612779A (fr)
CA (1) CA2245927A1 (fr)
EA (1) EA001436B1 (fr)
HU (1) HUP0000467A3 (fr)
IL (1) IL125717A0 (fr)
NO (1) NO983737L (fr)
NZ (1) NZ316710A (fr)
OA (1) OA10840A (fr)
PL (1) PL328562A1 (fr)
SK (1) SK110198A3 (fr)
TR (1) TR199801592T2 (fr)
WO (2) WO1996025157A1 (fr)

Families Citing this family (175)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11503110A (ja) * 1995-02-17 1999-03-23 スミスクライン・ビーチャム・コーポレイション Il−8受容体拮抗剤
US6054472A (en) * 1996-04-23 2000-04-25 Vertex Pharmaceuticals, Incorporated Inhibitors of IMPDH enzyme
US5807876A (en) 1996-04-23 1998-09-15 Vertex Pharmaceuticals Incorporated Inhibitors of IMPDH enzyme
US6211373B1 (en) * 1996-03-20 2001-04-03 Smithkline Beecham Corporation Phenyl urea antagonists of the IL-8 receptor
EP0914319B1 (fr) 1996-05-20 2001-11-21 Teijin Limited Derives de diamine cyclique de diarylaklyle utilises en tant qu'antagonistes des recepteurs de chimiokines
WO1997049399A1 (fr) * 1996-06-27 1997-12-31 Smithkline Beecham Corporation Antagonistes des recepteurs d'il-8
EP0934066A4 (fr) 1996-08-06 2001-10-17 Smithkline Beecham Corp Antagonistes du recepteur de l'interleukine-8 (il-8)
WO1998005317A1 (fr) * 1996-08-06 1998-02-12 Smithkline Beecham Corporation Antagonistes du recepteur de l'il-8
EP0939634A4 (fr) * 1996-08-15 2001-02-21 Smithkline Beecham Corp Antagonistes du recepteur il-8
AU3048797A (en) * 1996-10-22 1998-05-15 Chugai Seiyaku Kabushiki Kaisha Sepsis remedy comprising anti-il-8 antibody as active ingredient
DE19651040C2 (de) * 1996-12-09 1999-01-28 Bayer Ag Verfahren zur Herstellung von 2-Amino-5-alkyl-phenolen
CN1217660C (zh) 1997-01-23 2005-09-07 史密丝克莱恩比彻姆公司 Il-8受体拮抗剂
US6436927B1 (en) 1997-02-12 2002-08-20 Smithkline Beecham Corporation IL-8 receptor antagonists
JP2001512445A (ja) * 1997-02-12 2001-08-21 スミスクライン・ビーチャム・コーポレイション Il−8レセプターアンタゴニスト
US6696475B2 (en) 1997-04-22 2004-02-24 Neurosearch A/S Substituted phenyl derivatives, their preparation and use
US6344476B1 (en) * 1997-05-23 2002-02-05 Bayer Corporation Inhibition of p38 kinase activity by aryl ureas
EP1014962A4 (fr) * 1997-06-26 2007-06-27 Lilly Co Eli Agents antithrombotiques
JP2001512096A (ja) * 1997-07-29 2001-08-21 スミスクライン・ビーチャム・コーポレイション Il−8レセプターアンタゴニスト
US7067117B1 (en) 1997-09-11 2006-06-27 Cambridge University Technical Services, Ltd. Compounds and methods to inhibit or augment an inflammatory response
US6989435B2 (en) 1997-09-11 2006-01-24 Cambridge University Technical Services Ltd. Compounds and methods to inhibit or augment an inflammatory response
US7329670B1 (en) 1997-12-22 2008-02-12 Bayer Pharmaceuticals Corporation Inhibition of RAF kinase using aryl and heteroaryl substituted heterocyclic ureas
AU2003204708B2 (en) * 1997-12-22 2006-05-25 Bayer Healthcare Llc Inhibition of Raf Kinase using Substituted Heterocyclic Ureas
ATE291011T1 (de) * 1997-12-22 2005-04-15 Bayer Pharmaceuticals Corp Hemmung der raf-kinase unter verwendung von symmetrisch und unsymmetrisch substituierten harnstoffen
US7517880B2 (en) 1997-12-22 2009-04-14 Bayer Pharmaceuticals Corporation Inhibition of p38 kinase using symmetrical and unsymmetrical diphenyl ureas
JP4437270B2 (ja) * 1997-12-22 2010-03-24 バイエル コーポレイション 置換複素環式尿素を用いたrafキナーゼの阻害
US20080300281A1 (en) * 1997-12-22 2008-12-04 Jacques Dumas Inhibition of p38 Kinase Activity Using Aryl and Heteroaryl Substituted Heterocyclic Ureas
WO1999065310A1 (fr) * 1998-06-17 1999-12-23 Smithkline Beecham Corporation Antagonistes des recepteurs d'il-8
EP1098884A4 (fr) * 1998-07-23 2003-01-22 Smithkline Beecham Corp Antagonistes de recepteur d'il-8
WO2000012468A1 (fr) * 1998-08-28 2000-03-09 Smithkline Beecham Corporation Synthese amelioree de 3-hydroxy-4-amino-benzonitrile
EP1514867A3 (fr) * 1998-10-22 2005-03-23 NeuroSearch A/S Dérivés de phényle substitués, leur préparation et utilisation
US6201013B1 (en) 1998-12-09 2001-03-13 American Home Products Corporation Heterocyclic carboxamide-containing thiourea inhibitors of herpes viruses containing a substituted phenylenediamine group
US6197803B1 (en) 1998-12-09 2001-03-06 American Home Products Corporation Heterocyclic carboxamide-containing thiourea inhibitors of herpes viruses containing phenylenediamine group
US6262090B1 (en) 1998-12-09 2001-07-17 American Home Products Corporation Aminopyridine-containing thiourea inhibitors of herpes viruses
US6255349B1 (en) 1998-12-09 2001-07-03 American Home Products Corporation Alph-methylbenzyl-containing thiourea inhibitors of herpes viruses containing a phenylenediamine group
US6207715B1 (en) 1998-12-09 2001-03-27 American Home Products Corporation Alpha-methylbenzyl-containing thiourea inhibitors of herpes viruses containing a substituted phenylene-diamine group
ATE267824T1 (de) * 1998-12-09 2004-06-15 Wyeth Corp Alpha-methylbenzyl-enthaltende thioharnstoffe als inhibitoren von herpes-viren mit einer phenylenediamingruppe
US6166028A (en) 1998-12-09 2000-12-26 American Home Products Corporation Diaminopuridine-containing thiourea inhibitors of herpes viruses
US6335350B1 (en) 1998-12-09 2002-01-01 American Home Products Corporation Acetamide and substituted acetamide-containing thiourea inhibitors of herpes viruses
EP1137632B1 (fr) * 1998-12-09 2004-07-28 Wyeth Thio-urees inhibitrices des virus de l'herpes
US20080269265A1 (en) * 1998-12-22 2008-10-30 Scott Miller Inhibition Of Raf Kinase Using Symmetrical And Unsymmetrical Substituted Diphenyl Ureas
US7351834B1 (en) 1999-01-13 2008-04-01 Bayer Pharmaceuticals Corporation ω-Carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
US8124630B2 (en) 1999-01-13 2012-02-28 Bayer Healthcare Llc ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
EP2298311B1 (fr) * 1999-01-13 2012-05-09 Bayer HealthCare LLC Urées de diphényle à substitution omega-carboxyaryle en tant qu'inhibiteurs de la p38 kinase
EP1140840B1 (fr) * 1999-01-13 2006-03-22 Bayer Pharmaceuticals Corp. Diphenylurees a substituants -g(v)-carboxyaryles, inhibitrices de kinase raf
US7928239B2 (en) 1999-01-13 2011-04-19 Bayer Healthcare Llc Inhibition of RAF kinase using quinolyl, isoquinolyl or pyridyl ureas
UA73492C2 (en) 1999-01-19 2005-08-15 Aromatic heterocyclic compounds as antiinflammatory agents
MXPA01008440A (es) 1999-02-22 2002-04-24 Boehringer Ingelheim Pharma Derivados heterociclicos policiclos como agentes anti-inflamatorios..
TR200102817T2 (tr) 1999-03-12 2002-05-21 Boehringer Ingelheim Pharmaceuticals, Inc. Antiinflamatuar ajanlar olarak faydalı bileşikler
WO2000055152A1 (fr) * 1999-03-12 2000-09-21 Boehringer Ingelheim Pharmaceuticals, Inc. Composes aromatiques heterocycliques utilises en tant qu'agents anti-inflammatoires
EP1163212B1 (fr) * 1999-03-17 2005-08-31 AstraZeneca AB Derives amides
CO5170528A1 (es) * 1999-05-28 2002-06-27 Smithkline Beecham Corp Antagonistas de los receptores de la il-8 nistas del recpetor de la il-8
CO5190710A1 (es) * 1999-06-15 2002-08-29 Smithkline Beecham Corp Antagonistas de un receptor de il-8 un receptor de il-8
CO5200760A1 (es) * 1999-06-16 2002-09-27 Smithkline Beecham Corp Antagonistas del receptor de la il-8 ceptor il-8
KR20020029419A (ko) * 1999-07-07 2002-04-18 다비드 에 질레스 퀴나졸린 유도체
CA2374737C (fr) 1999-07-09 2008-02-12 Boehringer Ingelheim Pharmaceuticals, Inc. Nouveau procede de synthese de composes d'uree a substitution heteroaryle
EP1199306B1 (fr) 1999-07-26 2005-12-07 Banyu Pharmaceutical Co., Ltd. Derives de biaryluree
CO5271663A1 (es) * 1999-11-09 2003-04-30 Smithkline Beecham Corp Antagonistas del receptor il-8
ES2292488T3 (es) 1999-11-16 2008-03-16 Boehringer Ingelheim Pharmaceuticals Inc. Derivados de la urea, como agentes antiinflamatorios.
US6525046B1 (en) 2000-01-18 2003-02-25 Boehringer Ingelheim Pharmaceuticals, Inc. Aromatic heterocyclic compounds as antiinflammatory agents
US6608052B2 (en) 2000-02-16 2003-08-19 Boehringer Ingelheim Pharmaceuticals, Inc. Compounds useful as anti-inflammatory agents
EP1274413A4 (fr) * 2000-03-01 2005-08-10 Smithkline Beecham Corp Antagonistes du recepteur il-8
EP1261329A4 (fr) * 2000-03-10 2005-08-17 Smithkline Beecham Corp Antagonistes du recepteur de il-8
AR030273A1 (es) * 2000-03-10 2003-08-20 Smithkline Beecham Corp Compuestos de hidroxifenil urea sustituidos con sulfonamidas, composiciones farmaceuticas que los comprenden, y uso de los mismos en la fabricacion de medicamentos para tratar una enfermedad mediada por una quimioquina
EP1274415A4 (fr) * 2000-03-14 2005-09-07 Smithkline Beecham Corp Antagonistes du recepteur de il-8
CO5280089A1 (es) * 2000-03-16 2003-05-30 Smithkline Beecham Corp Antagonistas del receptor il-8
UY26627A1 (es) * 2000-03-24 2001-09-28 Smithkline Beecham Corp Antagonistas de receptores de il-8
CN1423635A (zh) * 2000-04-14 2003-06-11 吴羽化学工业株式会社 含氮化合物以及使用该化合物的抗病毒药
WO2001092202A1 (fr) * 2000-05-30 2001-12-06 Smithkline Beecham Corporation Antagonistes du recepteur de l'il-8
AU2001273497A1 (en) * 2000-07-18 2002-01-30 Smithkline Beecham Corporation Use of IL-8 receptor antagonists in the treatment of virus infections
AU2001290852A1 (en) * 2000-09-15 2002-03-26 Iconix Pharmaceuticals, Inc. Inhibitors of rho c
US7235576B1 (en) 2001-01-12 2007-06-26 Bayer Pharmaceuticals Corporation Omega-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
DE60230722D1 (de) * 2001-01-16 2009-02-26 Smithkline Beecham Corp Il-8-rezeptor-antagonisten
US20040048897A1 (en) * 2001-01-16 2004-03-11 Mccleland Brent Il-8 receptor antagonists
WO2002070467A1 (fr) 2001-02-26 2002-09-12 4Sc Ag Derives de diphenyluree, de diamide d'acide diphenyloxalique et de diamide d'acide diphenylsulfurique et leur utilisation comme medicaments
DE10109204A1 (de) * 2001-02-26 2002-09-19 4Sc Ag Verbindungen zur Behandlung von Protozoen-Erkrankungen
ITMI20010395A1 (it) * 2001-02-27 2002-08-27 Dompe Spa Omega-amminoalchilammidi di acidi r-2-aril-propionici come inibitori della chemiotassi di cellule polimorfonucleate e mononucleate
DK1379508T3 (da) 2001-02-28 2011-01-03 Univ Temple N-(aryl)-2arylethensulfonamider og terapeutiske anvendelser deraf
US7371763B2 (en) 2001-04-20 2008-05-13 Bayer Pharmaceuticals Corporation Inhibition of raf kinase using quinolyl, isoquinolyl or pyridyl ureas
US20040157818A1 (en) * 2001-05-24 2004-08-12 Mikiro Yanaka Cxcr4-antagonistic drugs composed of nitrogen-containing compound
US20040038854A1 (en) * 2001-07-16 2004-02-26 Dillon Susan B. Use of il-8 receptor antagonists in the treatment of virus infections
US6791892B2 (en) * 2001-07-18 2004-09-14 Samsung Electronics Co., Ltd. Method of generating an initializing signal during power-up of semiconductor memory device
EP2305255B1 (fr) * 2001-12-03 2012-08-22 Bayer HealthCare LLC Composes de type uree aryle combines a d'autres agents cytostatiques ou cytotoxiques et servant a traiter des cancers humains
US20080108672A1 (en) * 2002-01-11 2008-05-08 Bernd Riedl Omega-Carboxyaryl Substituted Diphenyl Ureas As Raf Kinase Inhibitors
WO2003068229A1 (fr) 2002-02-11 2003-08-21 Bayer Pharmaceuticals Corporation N-oxydes de pyridine, de quinoline, et d'isoquinoline en tant qu'inhibiteurs de kinase
ATE529406T1 (de) 2002-02-11 2011-11-15 Bayer Healthcare Llc Aryl-harnstoffe als kinase inhibitoren
DK1478358T3 (da) 2002-02-11 2013-10-07 Bayer Healthcare Llc Sorafenibtosylat til behandling af sygdomme kendetegnet ved unormal angiogenese
WO2003068223A1 (fr) * 2002-02-11 2003-08-21 Bayer Corporation Urees aryliques a kinase de raf et activite inhibitrice d'angiogenese
EP1480973B1 (fr) 2002-02-25 2008-02-13 Boehringer Ingelheim Pharmaceuticals Inc. Composes de cycloalkyle uree benzofusionnes a disubstitution en position 1,4 utiles dans le traitement de maladies mediees par la cytokine
IL163608A0 (en) * 2002-02-28 2005-12-18 Univ Temple Amino-substituted sulfonanilides and derivatives thereof for treating proliferative disorders
KR20030080509A (ko) * 2002-04-09 2003-10-17 주식회사 엘지생명과학 우레아, 티오우레아 및 설파마이드 유도체를 함유하는항균제 조성물
US20030236287A1 (en) * 2002-05-03 2003-12-25 Piotrowski David W. Positive allosteric modulators of the nicotinic acetylcholine receptor
CA2493253A1 (fr) * 2002-08-01 2004-02-12 Neurosearch A/S Composes utilises dans le traitement de maladies sensibles a une therapie anti-angiogenetique
KR100863667B1 (ko) * 2002-09-11 2008-10-15 가부시끼가이샤 구레하 아민 화합물 및 그 용도
EP1402887A1 (fr) * 2002-09-18 2004-03-31 Jerini AG Nouvelles composés pour inhibiter la prolifération non-désirée des cellules, et leurs utilisation
AR041834A1 (es) * 2002-10-29 2005-06-01 Smithkline Beecham Corp Compuesto de difenilurea sustituido con sulfonamida, composicion farmaceutica que lo comprende y su uso para preparar dicha composicion
DE10251830A1 (de) * 2002-11-07 2004-05-19 Wella Ag 2-Amino-5-ethylphenol enthaltendes Mittel zum Färben von Keratinfasern
US7521480B2 (en) 2002-11-21 2009-04-21 Neurosearch Aryl ureido benzoic acid derivatives and their use
US20040198777A1 (en) * 2002-12-20 2004-10-07 Mitokor, Inc. Ligands of adenine nucleotide translocase (ANT) and compositions and methods related thereto
WO2004058722A1 (fr) * 2002-12-24 2004-07-15 Arena Pharmaceuticals, Inc. Derives du pyrazole diarylamine et du pyrazole arylheteroarylamine modulateurs du 5ht2a
US7220768B2 (en) * 2003-02-11 2007-05-22 Wyeth Holdings Corp. Isoxazole-containing thiourea inhibitors useful for treatment of varicella zoster virus
US7874293B2 (en) * 2003-02-21 2011-01-25 Resmed Limited Nasal assembly
UY28213A1 (es) 2003-02-28 2004-09-30 Bayer Pharmaceuticals Corp Nuevos derivados de cianopiridina útiles en el tratamiento de cáncer y otros trastornos.
EP1457485A1 (fr) * 2003-03-14 2004-09-15 Dompé S.P.A. Acides sulfoniques, leurs dérivés ainsi que compositions pharmaceutiques les contenants
WO2004089296A2 (fr) * 2003-04-03 2004-10-21 The Regents Of The University Of California Inhibiteurs ameliores pour hydrolase epoxyde soluble
EP1636585B2 (fr) 2003-05-20 2012-06-13 Bayer HealthCare LLC Diaryl-urees presentant une activite d'inhibition des kinases
NZ544331A (en) 2003-07-22 2010-03-26 Arena Pharm Inc Diaryl and arylheteroaryl urea derivatives as modulators of the 5-HT2A serotonin receptor useful for the prophylaxis and treatment of disorders related thereto
PL1663978T3 (pl) 2003-07-23 2008-04-30 Bayer Healthcare Llc Fluoropodstawiony omega-karboksyarylodifenylomocznik do leczenia i profilaktyki chorób i stanów
CN1845726A (zh) 2003-09-04 2006-10-11 波塞东医药公司 用于治疗心脏心律失常的erg通道开放剂
WO2005023238A1 (fr) * 2003-09-04 2005-03-17 Poseidon Pharmaceuticals A/S Ouvreurs du canal erg destines au traitement de maladies neuronales liees a l'hyperexcitabilite
TW200530236A (en) 2004-02-23 2005-09-16 Chugai Pharmaceutical Co Ltd Heteroaryl phenylurea
KR101149124B1 (ko) * 2004-03-10 2012-05-25 가부시끼가이샤 구레하 아민계 염기성 화합물과 그의 용도
EP1765311A4 (fr) 2004-03-16 2009-04-29 Univ California Reduction de la nephropathie au moyen d'inhibiteurs d'hydrolase d'epoxyde soluble et d'epoxyeicosanoides
CN1926114B (zh) * 2004-03-23 2011-08-24 艾尼纳制药公司 用于制备经取代n-芳基-n′-′3-(1h-吡唑-5-基)苯基脲及其中间体的方法
AU2005225559A1 (en) * 2004-03-29 2005-10-06 Neurosearch A/S Novel urea derivatives and their medical use
US7838524B2 (en) 2004-04-30 2010-11-23 Bayer Healthcare Llc Substituted pyrazolyl urea derivatives useful in the treatment of cancer
CN1984899B (zh) * 2004-05-12 2011-07-27 先灵公司 Cxcr1和cxcr2趋化因子拮抗剂
US7550499B2 (en) 2004-05-12 2009-06-23 Bristol-Myers Squibb Company Urea antagonists of P2Y1 receptor useful in the treatment of thrombotic conditions
AU2005245389A1 (en) * 2004-05-12 2005-12-01 Bristol-Myers Squibb Company Urea antagonists of P2Y1 receptor useful in the treatment of thrombotic conditions
FR2872159B1 (fr) * 2004-06-28 2007-10-05 Merck Sante Soc Par Actions Si Nouveaux derives acides carboxyliques phenyliques et leur utilisation dans le traitement du diabete
AU2005273612B2 (en) 2004-08-12 2010-10-14 Pfizer Inc. Triazolopyridinylsulfanyl derivatives as p38 map kinase inhibitors
EP1634573A1 (fr) * 2004-08-16 2006-03-15 The Procter and Gamble Company Composés 2-(Amino ou amino substitué)-5-6-substituée de phenol, compositions les contenant et leur utilisation
CN101039652A (zh) * 2004-08-16 2007-09-19 宝洁公司 2-(氨基或取代的氨基)-5,6-取代的苯酚化合物,包含该化合物的染料组合物以及它们的应用
WO2006043950A1 (fr) * 2004-10-20 2006-04-27 Smithkline Beecham Corporation Antagonistes du récepteur il-8
WO2006045119A2 (fr) * 2004-10-20 2006-04-27 The Regents Of The University Of California Inhibiteurs ameliores de l'epoxyde hydrolase soluble
EP1809619A1 (fr) 2004-10-21 2007-07-25 Transtech Pharma, Inc. Composes bissulfonamide utilises en tant qu'agonistes du galr1, compositions, et procedes d'utilisation associes
PE20061130A1 (es) * 2004-11-19 2007-01-05 Arena Pharm Inc Derivados de 3-fenil-pirazol como moduladores del receptor de serotonina 5-ht2a
WO2006060762A2 (fr) * 2004-12-03 2006-06-08 Arena Pharmaceuticals, Inc. Derives de pyrazole en tant que modulateurs du recepteur de serotinine 5-ht2a utiles dans le traitement de troubles associes a ce recepteur
CA2594563A1 (fr) * 2005-01-19 2006-07-27 Arena Pharmaceuticals, Inc. Derives de diaryl-uree et d'arylheteroaryl-uree utilises comme modulateurs du recepteur de la serotonine 5-ht2a et utiles pour la prevention ou le traitement de la leucoencephalopathie multifocale progressive
MX2007008434A (es) 2005-01-19 2007-07-25 Squibb Bristol Myers Co Derivados de 2-fenoxi-n-(1,3,4-tiadizol-2il)piridin-3-amina y compuestos relacionados como inhibidores del receptor p2y1 para el tratamiento de trastornos tromboembolicos.
US20090305321A1 (en) * 2005-03-23 2009-12-10 Astrazeneca Ab Assays for Allosteric Modulators of G-Protein Coupled Receptors (GPCRs)
WO2007002634A1 (fr) 2005-06-27 2007-01-04 Bristol-Myers Squibb Company Antagonistes carbocycliques et heherocycliques du recepteur p2y1, utiles pour traiter des etats pathologiques thrombotiques
AR056867A1 (es) 2005-06-27 2007-10-31 Bristol Myers Squibb Co Antagonistas heterociclicos n- enlazados del receptor de p2y1 utiles en el tratamiento de condiciones tromboticas. composiciones farmaceuticas.
WO2007002584A1 (fr) 2005-06-27 2007-01-04 Bristol-Myers Squibb Company Mimetiques lineaires de l’uree antagonistes du recepteur p2y1, utilises dans le traitement des troubles thrombotiques
ATE485269T1 (de) 2005-06-27 2010-11-15 Bristol Myers Squibb Co C-verknüpfte zyklische antagonisten des p2y1- rezeptors mit eignung bei der behandlung thrombotischer leiden
GB0526255D0 (en) 2005-12-22 2006-02-01 Novartis Ag Organic compounds
CA2640090A1 (fr) * 2006-01-25 2007-08-02 Synta Pharmaceuticals Corp. Composes aromatiques substitues destines a des utilisations contre des inflammations et des troubles immunitaires
MX2008013600A (es) * 2006-04-21 2008-10-31 Smithkline Beechman Corp Antagonistas del receptor de interleuquina-8.
CA2650007A1 (fr) * 2006-04-21 2007-11-01 Smithkline Beecham Corporation Antagonistes du recepteur de l'il-8
WO2007127930A2 (fr) * 2006-04-28 2007-11-08 Kansas State University Research Foundation Composés pour influencer une activité de jonctions lacunaires
US8148417B2 (en) * 2006-05-18 2012-04-03 Arena Pharmaceuticals, Inc. Primary amines and derivatives thereof as modulators of the 5-HT2A serotonin receptor useful for the treatment of disorders related thereto
EP2027119A2 (fr) * 2006-05-18 2009-02-25 Arena Pharmaceuticals, Inc. Éthers, amines secondaires et leurs dérivés utilisés en tant que modulateurs des récepteurs 5-ht2a de la sérotonine et utiles pour traiter les troubles liés à ces récepteurs
NZ571829A (en) 2006-05-18 2011-10-28 Arena Pharm Inc Crystalline forms and processes for the preparation of phenyl-pyrazoles useful as modulators of the 5-HT2A serotonin receptor
CL2007001829A1 (es) * 2006-06-23 2008-01-25 Smithkline Beecham Corp P-toluensulfonato de n-[4-cloro-2-hidroxi-3-(piperazina-1-sulfonil)fenil]-n-(2-cloro-3-fluorofenil)urea;procedimiento de preparacion;composicion farmaceutica;combinacion farmaceutica;y uso en el tratamiento de una enfermedad mediada por la quiimioquina il-8, tales como asma y epoc.
TWI415845B (zh) 2006-10-03 2013-11-21 Arena Pharm Inc 用於治療與5-ht2a血清素受體相關聯病症之作為5-ht2a血清素受體之調節劑的吡唑衍生物
US7960569B2 (en) 2006-10-17 2011-06-14 Bristol-Myers Squibb Company Indole antagonists of P2Y1 receptor useful in the treatment of thrombotic conditions
WO2008047067A1 (fr) * 2006-10-20 2008-04-24 University Court Of The University Of Edinburgh Traitement d'une maladie inflammatoire
ES2421237T7 (es) 2007-08-15 2013-09-30 Arena Pharmaceuticals, Inc. Derivados de imidazo[1,2-a]piridin como moduladores del receptor serotoninérgico 5ht2a en el tratamiento de trastornos relacionados con el mismo
US20100305207A1 (en) * 2007-09-28 2010-12-02 Pierette Banker Glycogen phosphorylase inhibitor compound and pharmaceutical composition thereof
WO2009123714A2 (fr) * 2008-04-02 2009-10-08 Arena Pharmaceuticals, Inc. Procédés de préparation de dérivés de pyrazole utiles comme modulateurs du récepteur de la sérotonine 5-ht<sb>2a</sb>
US9126946B2 (en) 2008-10-28 2015-09-08 Arena Pharmaceuticals, Inc. Processes useful for the preparation of 1-[3-(4-bromo-2-methyl-2H-pyrazol-3-yl)-4-methoxy-phenyl]-3-(2,4-difluoro-phenyl)urea and crystalline forms related thereto
TR201805216T4 (en) 2008-10-28 2018-06-21 Arena Pharm Inc COMPOSITIONS OF A USEFUL 5-HT2A SEROTONINE RECEPTOR MODULATOR FOR THE TREATMENT OF RELATED DISORDERS
WO2010092440A1 (fr) * 2009-02-16 2010-08-19 Inserm (Institut National De La Sante Et De La Recherche Medicale) Antagonistes du récepteur cxcr2 pour le traitement ou la prévention de la résistance à l'insuline
WO2011022028A2 (fr) * 2009-05-18 2011-02-24 Tufts University Antagonistes à petites molécules de phosphatidylinositol-3, 4, 5-triphosphate (pip3) et ses utilisations
EP2512465A1 (fr) * 2009-12-17 2012-10-24 Galderma Research & Development Utilisation de composés dans traitement ou prévention d'affections cutanées
US8980891B2 (en) 2009-12-18 2015-03-17 Arena Pharmaceuticals, Inc. Crystalline forms of certain 3-phenyl-pyrazole derivatives as modulators of the 5-HT2A serotonin receptor useful for the treatment of disorders related thereto
BRPI1004176A2 (pt) * 2010-10-25 2015-08-11 Univ Rio De Janeiro Compostos aril e/ou hetero aril uréias funcionalizados; processo de síntese desses composto; composição farmacêutica contendo tais compostos e usos
US8648118B2 (en) 2010-12-17 2014-02-11 Boehringer Ingelheim International Gmbh Bicyclic ring system substituted amide functionalised phenols as medicaments
WO2012149540A1 (fr) 2011-04-28 2012-11-01 The Broad Institute Inc Inhibiteurs de l'histone désacétylase
EP2877444B1 (fr) 2012-07-27 2020-09-02 The Broad Institute, Inc. Inhibiteurs d'histone-désacétylases
CN104797429B (zh) * 2012-11-21 2017-04-19 日本曹达株式会社 使用非酚类化合物的记录材料、记录片和将非酚类化合物用于显色剂的方法
US9914717B2 (en) 2012-12-20 2018-03-13 The Broad Institute, Inc. Cycloalkenyl hydroxamic acid derivatives and their use as histone deacetylase inhibitors
CN104995033B (zh) * 2013-02-13 2017-10-13 王子控股株式会社 热敏记录体
EP3000608B1 (fr) * 2013-05-22 2020-03-18 Oji Holdings Corporation Support d'enregistrement thermosensible
JP2018516992A (ja) 2015-06-12 2018-06-28 アクソファント サイエンシーズ ゲーエムベーハーAxovant Sciences Gmbh レム睡眠行動障害の予防および処置のために有用なジアリールおよびアリールヘテロアリール尿素誘導体
EP3117835A1 (fr) * 2015-07-14 2017-01-18 Dompé farmaceutici s.p.a. Inhibiteurs il-8 pour utilisation dans le traitement de certains troubles urologiques
CN108472285A (zh) 2015-07-15 2018-08-31 阿速万科学有限责任公司 用于预防和治疗与神经退行性疾病相关联的幻觉的二芳基和芳基杂芳基脲衍生物
US10093617B1 (en) 2015-10-30 2018-10-09 Sumitomo Chemical Company, Limited Method for producing 2-amino-4-substituted phenol
WO2017219935A1 (fr) * 2016-06-22 2017-12-28 复旦大学 Dérivé de biaryle urée ou son sel, sa fabrication et son application
CN107522641B (zh) * 2016-06-22 2020-05-05 复旦大学 联芳基脲类衍生物或其盐及其制备方法和用途
WO2018067548A1 (fr) 2016-10-03 2018-04-12 The Children's Medicial Center Corporation Prévention et traitement de néphropathie diabétique
CA3125731A1 (fr) 2018-01-12 2019-07-18 KDAc Therapeutics, Inc. Combinaison d'un inhibiteur selectif de desacetylase d'histone 3 (hdac3) et d'un agent d'immunotherapie pour le traitement du cancer
CN110698373A (zh) * 2019-11-07 2020-01-17 温州大学 N-(2-(甲硫基)苯基)乙酰胺类化合物的制备方法及其净化提纯方法
CN112321452B (zh) * 2020-09-11 2022-11-29 北京红惠新医药科技有限公司 厚朴酚衍生物、和厚朴酚衍生物及其盐酸盐、制备方法及应用
WO2025121190A1 (fr) * 2023-12-08 2025-06-12 日産化学株式会社 Polymère, composition de résine, agent d'alignement de cristaux liquides, film de revêtement en résine et film d'alignement de cristaux liquides
CN118063332A (zh) * 2024-02-29 2024-05-24 浙江鼎龙科技股份有限公司 一种2-羟基-4-乙基苯胺及其盐酸盐的制备方法

Family Cites Families (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2363074A (en) * 1938-06-16 1944-11-21 Geigy Ag J R Halogen substituted acylamino sulphonic acids of the aromatic series and their manufacture
US3332981A (en) * 1964-09-14 1967-07-25 Gen Aniline & Film Corp Urea stilbene brighteners
US3996253A (en) * 1966-01-11 1976-12-07 Minnesota Mining And Manufacturing Company Process for the preparation of color images
GB1210596A (en) * 1967-04-06 1970-10-28 Armour Grocery Products Compan Antiseptic compositions
CH506240A (de) * 1969-02-04 1971-04-30 Ciba Geigy Ag Verwendung von N-Hydroxyphenyl-N'-phenylharnstoffen zur Bekämpfung schädlicher Mikroorganismen ausserhalb der Textilindustrie
SE370866B (fr) * 1968-03-21 1974-11-04 Ciba Geigy Ag
GB1281437A (en) * 1970-07-23 1972-07-12 Ici Ltd Urea derivatives
US3855285A (en) * 1971-06-21 1974-12-17 Pfizer Acylmethylthio-trifluoromethyl-benzoic acids
US3856951A (en) * 1971-06-21 1974-12-24 Co Pfizer Inc Substituted benzoic acid hypoliphemic agents
DE2241470A1 (de) * 1971-08-23 1973-03-22 Midizinska Akademia Arzneimittel mit antivirus-wirksamkeit
US4048333A (en) * 1971-08-23 1977-09-13 Medizinska Akademia Method for treating a picorna virus infection
US3882230A (en) * 1972-11-07 1975-05-06 Pfizer Substituted benzoic acid hypolipemic agents
US3869553A (en) * 1972-11-07 1975-03-04 Pfizer Substituted benzoic acid hypolipemic agents
GB1393854A (en) * 1973-02-26 1975-05-14 Pfizer Benzoic acid compounds and pharmaceutical compositions containing them
JPS5598152A (en) * 1979-01-16 1980-07-25 Hokko Chem Ind Co Ltd Phenylurea derivative
DE2928485A1 (de) * 1979-07-14 1981-01-29 Bayer Ag Verwendung von harnstoffderivaten als arzneimittel bei der behandlung von fettstoffwechselstoerungen
DE2942930A1 (de) * 1979-10-24 1981-05-27 Basf Ag, 6700 Ludwigshafen Substituierte harnstoffe, deren herstellung und verwendung als herbizide
DE3006671A1 (de) * 1980-02-22 1981-08-27 Dr. Karl Thomae Gmbh, 7950 Biberach Neue benzoxazole, deren herstellung und deren verwendung als arzneumittel
US4608205A (en) * 1983-03-09 1986-08-26 American Cyanamid Company Polyanionic benzene ureas
JPS60126256A (ja) * 1983-12-13 1985-07-05 Hokko Chem Ind Co Ltd Ν−アシルクロルアミノフエノ−ル誘導体
US4591604A (en) * 1984-03-28 1986-05-27 American Cyanamid Company Method of inhibiting the complement system by administering multisulfonated naphthalene ureas
DD253997A1 (de) * 1986-11-26 1988-02-10 Karl Marx Uni Buero Fuer Neuer Verfahren zur herstellung von substituierten 2-arylureidophenolen
JP2684409B2 (ja) * 1988-03-31 1997-12-03 コニカ株式会社 シアノ基および/またはハロゲン原子で置換されたアニリン類の製造方法およびその製造のために使用される化合物
JP2835631B2 (ja) * 1990-01-19 1998-12-14 コニカ株式会社 色再現性の改良されたハロゲン化銀カラー写真感光材料
US5276182A (en) * 1990-07-09 1994-01-04 The Dow Chemical Company Process for preparing polyurea oligomers
JP2655384B2 (ja) * 1991-11-08 1997-09-17 富士写真フイルム株式会社 ポジ型レジスト組成物
DE4200259A1 (de) * 1992-01-08 1993-07-15 Asta Medica Ag Neue 1,2,4-triaminobenzol-derivate und verfahren zu deren herstellung
US5424063A (en) * 1992-01-09 1995-06-13 The Dow Chemical Company Narrow poly- and mono-dispersed anionic oligomers, and their uses, formulations and process
JP3264492B2 (ja) * 1992-01-13 2002-03-11 スミスクライン・ビーチャム・コーポレイション ピリジル置換イミダゾール
JP3309104B2 (ja) * 1992-02-20 2002-07-29 メレルダウファーマス−ティカルズ インコーポレイテッド ウイルス病治療用のスルホン酸誘導体類
US5275932A (en) * 1992-03-16 1994-01-04 Minnesota Mining And Manufacturing Company Thermal development accelerators for thermographic materials
KR950703347A (ko) * 1992-09-28 1995-09-20 스티븐 엘. 네스비트 이노시톨 1,4,5-트리포스페이트의 길항 방법(Method for Antagonizing Inositol 1,4,5-Triphosphate)
US5384319A (en) * 1993-01-06 1995-01-24 Ciba-Geigy Corporation Aminoalkylphenyl compounds
DK41193D0 (da) * 1993-04-07 1993-04-07 Neurosearch As Ionkanalaabnere
JPH06313992A (ja) * 1993-04-28 1994-11-08 Canon Inc 静電荷像現像用トナー
US5312831A (en) * 1993-05-12 1994-05-17 American Cyanamid Company Urethanes and ureas that induce cytokine production
CA2123728A1 (fr) * 1993-05-21 1994-11-22 Noriyoshi Sueda Derives de l'uree et leur utilisation comme inhibiteurs de l'acat
IL110296A (en) * 1993-07-16 1999-12-31 Smithkline Beecham Corp Imidazole compounds process for their preparation and pharmaceutical compositions containing them
DE4413265A1 (de) * 1994-04-16 1995-10-19 Basf Ag Hydroxyphenylharnstoffe
US5470882A (en) * 1994-06-02 1995-11-28 Smithkline Beecham Corp. Anti-inflammatory compounds
US5447957A (en) * 1994-06-02 1995-09-05 Smithkline Beecham Corp. Anti-inflammatory compounds
JPH10506339A (ja) * 1994-09-27 1998-06-23 イメイション・コーポレイション レーザーアドレス可能な熱転写要素
JPH11503110A (ja) * 1995-02-17 1999-03-23 スミスクライン・ビーチャム・コーポレイション Il−8受容体拮抗剤
SE506240C2 (sv) 1996-03-04 1997-11-24 Laxo Mekan Ab Sidofäste för snöplogsblad

Similar Documents

Publication Publication Date Title
JP2000500033A5 (fr)
JP2000500228A5 (fr)
JP2000500445A5 (fr)
JPH11514289A5 (fr)
JP2000500327A5 (fr)
JPH11510779A5 (fr)
JP2000500155A5 (fr)
JP2000500406A5 (fr)
JPH11507746A5 (fr)
JP2000500361A5 (fr)
JP2000500115A5 (fr)
JP2000500322A5 (fr)
JP2000500258A5 (fr)
JP2000500342A5 (fr)
JP2000500112A5 (fr)
JPH11507655A5 (fr)
JP2000500166A5 (fr)
JP2000500051A5 (fr)
JP2000500397A5 (fr)
JP2000500407A5 (fr)
JP2000500019A5 (fr)
JP2000500125A5 (fr)
JP2000500044A5 (fr)
JP2000500346A5 (fr)
JP2000500257A5 (fr)